Preparation of acariogenic sugar substitutes

ABSTRACT

The invention relates to sucrose isomerases, to DNA sequences that code for sucrose isomerases, and to novel processes for the production of non-cariogenic sugars.

This is a divisional of U.S. application Ser. No. 10/061,269, filed Feb. 4, 2002, now U.S. Pat. No. 6,884,611 B1, which is a continuation-in-part of U.S. application Ser. No. 09/168,720, filed Oct. 9, 1998, now abandoned, which is a divisional of U.S. application Ser. No. 08/785,396, now U.S. Pat. No. 5,985,622, filed Jan. 21, 1997, which is a divisional of U.S. application Ser. No. 08/374,155, now U.S. Pat. No. 5,786,140, filed Jan. 18, 1995, which claims priority of DE P 44 01 451.1, filed Jan. 19, 1994 and DE 44 14 185.8, filed Apr. 22, 1994. All of these documents are expressly incorporated by reference. All patents and other publications listed herein are expressly incorporated by reference.

The present invention relates to an improved process for the preparation of non-cariogenic sugars, in particular trehalulose and/or palatinose, using recombinant DNA technology.

The acariogenic sugar substitutes palatinose (isomaltulose) and trehalulose are produced on a large scale from sucrose by an enzymatic rearrangement using immobilized bacterial cells (for example of the species Protaminobacter rubrum, Erwinia rhapontici, Serratia plymuthica). This entails the α1→β2 glycosidic linkage existing between the two monosaccharide units of the disaccharide sucrose being isomerized to an α1→6 linkage in palatinose and to an α1→α1 linkage in trehalulose. This rearrangement of sucrose to give the two acariogenic disaccharides takes place with catalysis by the bacterial enzyme sucrose isomerase, also called sucrose mutase. Depending on the organism used, this reaction results in a product mixture which, besides the desired acariogenic disaccharides palatinose and trehalulose, also contains certain proportions of unwanted monosaccharides (glucose and/or fructose). These monosaccharide contents are a considerable industrial problem because elaborate purification procedures (usually fractional crystallizations) are necessary to remove them.

For example EP-0 028 900 describes a method for producing palantinose in a bioreactor by using immobilized sucrose isomerase, which was purified and immobilized from a raw extract by selectively binding to an anionic carrier matrix. The product composition obtained by this method contains, apart from the desired acariogenic disaccharides palantinose and trehalulose, 2.1–2.5% of the unwanted monosaccharide fructose and 0.6–1.0% of the unwanted monosaccharide glucose.

Further, EP-0 483 755 describes a method for producing trehalulose and palatinose, wherein a sucrose solution is contacted with at least one trehalulose-forming enzyme system of a trehalulose-forming microorganism at a temperature of 10–35° C., wherein a mostly tetrahalulose-containing product mixture is obtained, which, however, contains low amounts of the unwanted monosaccharides fructose and glucose. It could further be shown that the amount of unwanted monosaccharides drastically increases by using higher incubation temperatures preferred in large-scale technical methods and, in addition, a rapid thermal inactivation of the enzyme preparations occurred.

One object on which the present invention is based was thus to suppress as far as possible the formation of monosaccharides in the isomerization of sucrose to trehalulose and/or palatinose. Another object on which the present invention is based was to provide organisms which produce palatinose and/or trehalulose in a higher yield than do known organisms.

To achieve these objects, recombinant DNA molecules, organisms transformed with recombinant DNA molecules, recombinant proteins and an improved process for the preparation of non-cariogenic sugars, in particular of palatinose and/or trehalulose, are provided.

The invention relates to a DNA sequence which codes for a protein with a sucrose isomerase activity and comprises

-   -   (a) one of the nucleotide sequences shown in SEQ ID NO:1, SEQ ID         NO:2, SEQ ID NO:3, SEQ ID NO:9, SEQ ID NO:11 or SEQ ID NO:13,         where appropriate without the signal peptide-coding region,     -   (b) a nucleotide sequence corresponding to the sequences         from (a) within the scope of the degeneracy of the genetic code,         or     -   (c) a nucleotide sequence which hybridizes with the sequences         from (a) and/or (b).

In the context of the present invention, the term “protein with a sucrose isomerase activity” is intended to embrace those proteins which are able to isomerize sucrose to other disaccharides with conversion of the α1→β2 glycosidic linkage between glucose and fructose in sucrose into another glycosidic linkage between two monosaccharide units, in particular into an α1→6 linkage and/or an α1→α1 linkage. The term “protein with a sucrose isomerase activity” therefore particularly preferably relates to a protein which is able to isomerize sucrose to palatinose and/or trehalulose. Moreover, the proportion of palatinose and trehalulose in the total disaccharides formed by isomerization of sucrose is preferably ≧2%, particularly preferably ≧20% and most preferably ≧50%.

The nucleotide sequence shown in SEQ ID NO:1 codes for the complete sucrose isomerase from the microorganism Protaminobacter rubrum (CBS 547.77) including the signal peptide region. The nucleotide sequence shown in SEQ ID NO:2 codes for the N-terminal section of the sucrose isomerase from the microorganism Erwinia rhapontici (NCPPB 1578) including the signal peptide region. The nucleotide sequence shown in SEQ ID NO:3 codes for a section of the sucrose isomerase from the microorganism SZ 62 (Enterobacter spec.).

The region which codes for the signal peptide in SEQ ID NO:1 extends from nucleotide 1–99. The region coding for the signal peptide in SEQ ID NO:2 extends from nucleotide 1–108. The DNA sequence according to the present invention also embraces the nucleotide sequences shown in SEQ ID NO:1 and SEQ ID NO:2 without the region coding for the signal peptide because the signal peptide is, as a rule, necessary only for correct localization of the mature protein in a particular cell compartment (for example in the periplasmic space between the outer and inner membrane, in the outer membrane or in the inner membrane) or for extracellular export, but not for the enzymatic activity as such. The present invention thus furthermore embraces sequences which also code for the mature protein (without signal peptide) and are operatively linked to heterologous signal sequences, in particular to prokaryotic signal sequences as described, for example, in E. L. Winnacker, Gene und Klone, Eine Einführung in die Gentechnologie, VCH-Verlagsgesellschaft Weinheim, Germany (1985), p. 256.

Nucleotide sequence SEQ ID NO:9 codes for a variant of the isomerase from Protaminobacter rubrum. Nucleotide sequence SEQ ID NO:11 codes for the complete isomerase from the isolate SZ 62. Nucleotide, sequence SEQ ID NO:13 codes for most of the isomerase from the microorganism MX-45 (FERM 11808 or FERM BP 3619).

Besides the nucleotide sequences shown in SEQ ID NO:1 SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:9, SEQ ID NO:11 or SEQ ID NO:13, and nucleotide sequences corresponding to one of these sequences within the scope of the degeneracy of the genetic code, the present invention also embraces a DNA sequence which hybridizes with one of these sequences, provided that it codes for a protein which is able to isomerize sucrose. The term “hybridization” according to the present invention is used as in Sambrook et al. (Molecular Cloning. A Laboratory Manual, Cold Spring Harbor Laboratory Press (1989), 1.101–1.104). According to the present invention, hybridization is the word used when a positive hybridization signal is still observed after washing for 1 hour with 1×SSC and 0.1% SDS at 55° C., preferably at 62° C. and particularly preferably at 68° C., in particular for 1 hour in 0.2×SSC and 0.1% SDS at 55° C., preferably at 62° C. and particularly preferably at 68° C. A nucleotide sequence which hybridizes under such washing conditions with one of the nucleotide sequences shown in SEQ ID NO:1 or SEQ ID NO:2, or with a nucleotide sequence which corresponds thereto within the scope of the degeneracy of the genetic code, is a nucleotide sequence according to the invention.

The DNA sequence according to the invention preferably has

-   -   (a) one of the nucleotide sequences shown in SEQ ID NO:1, SEQ ID         NO:2, SEQ ID NO:3, SEQ ID NO:9, SEQ ID NO:11 or SEQ ID NO:13,         where appropriate without the signal peptide-coding region, or     -   (b) a nucleotide sequence which is at least 70% homologous with         the sequences from (a).

The DNA sequence according to the invention preferably also has an at least 80% homologous nucleotide sequence to the conserved part-regions of the nucleotide sequences shown in SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:9, SEQ ID NO:11 or SEQ ID NO:13. These conserved part-regions are, in particular, from nucleotide 139–186, nucleotide 256–312, nucleotide 328–360, nucleotide 379–420 and/or nucleotide 424–444 in the nucleotide sequence shown in SEQ ID NO:1.

In a particularly preferred embodiment, the DNA sequence according to the invention has an at least 80% homologous, in particular an at least 90% homologous, nucleotide sequence to the part-regions

-   -   (a) nucleotide 139–155 and/or     -   (b) nucleotide 625–644         of the nucleotide sequence shown in SEQ ID NO:1.

Oligonucleotides derived from the above sequence regions have proved suitable as primers for PCR amplification of isomerase fragments from the genomic DNA of a large number of tested microorganisms, for example Protaminobacter rubrum (CBS 547.77), Erwinia rhapontici (NCPPB 1578), isolate SZ 62 and Pseudomonas mesoacidophila MX-45 (FERM 11808).

Particularly preferably used for this purpose are the following oligonucleotides, where appropriate in the form of mixtures, where the bases in parentheses can be present as alternatives:

Oligonucleotide I (17 nt): 5-′TGGTGGAA(A,G)GA(G,A)GCTGT-3′ (SEQ ID NO:17) Oligonucleotide II (20 nt): 5′-TCCCAGTTCAG(G,A)TCCGGCTG-3′ (SEQ ID NO:18)

Oligonucleotide I is derived from nucleotides 139–155 of SEQ ID NO:1, and oligonucleotide II is derived from the sequence, complementary to nucleotides 625–644, of SEQ ID NO:1. The differences between the homologous part-regions of the DNA sequences according to the invention and the sequences called oligonucleotide I and oligonucleotide II are preferably in each case not more than 2 nucleotides and particularly preferably in each case not more than 1 nucleotide.

In another particularly preferred embodiment of the present invention, the DNA sequence has an at least 80% homologous, in particular an at least 90% homologous, nucleotide sequence to the part-regions of

-   -   (c) nucleotide 995–1013 and/or     -   (d) nucleotide 1078–1094         of the nucleotide sequence shown in SEQ ID NO:1.

Oligonucleotides derived from the above sequence regions hybridize with sucrose isomerase genes from the organisms Protaminobacter rubrum and Erwinia rhapontici. The following oligonucleotides, where appropriate in the form of mixtures, are particularly preferably used, where the bases indicated in parentheses may be present as alternatives:

Oligonucleotide III (19 nt): AAAGATGGCG(G,T)CGAAAAGA (SEQ ID NO:19) oligonucleotide IV (17 nt): 5′-TGGAATGCCTT(T,C)TTCTT-3′ (SEQ ID NO:20)

Oligonucleotide III is derived from nucleotides 995–1013 of SEQ ID NO:1, and oligonucleotide IV is derived from nucleotides 1078–1094 of SEQ ID NO:1. The differences between the homologous part-regions of the DNA sequences according to the invention and the sequences called oligonucleotide III and IV are preferably in each case not more than 2 nucleotides and particularly preferably in each case not more than 1 nucleotide.

Nucleotide sequences according to the invention can be obtained in particular from microorganisms of the genera Protaminobacter, Erwinia, Serratia, Leuconostoc, Pseudomonas, Agrobacterium and Klebsiella. Specific examples of such microorganisms are Protoaminobacter rubrum (CBS 547.77), Erwinia rhapontici (NCPPB 1578), Serratia plymuthica (ATCC 15928), Serratia marcescens (NCIB 8285), Leuconostoc mesenteroides NRRL B-521f (ATCC 10830a), Pseudomonas mesoacidophila MX-45 (FERM 11808 or FERM BP 3619), Agrobacterium radiobacter MX-232 (FERM 12397 or FERM BP 3620), Klebsiella subspecies and Enterobacter species. The nucleotide sequences according to the invention can be isolated in a simple manner from the genome of the relevant microorganisms, for example using oligonucleotides from one or more of the conserved regions of SEQ ID NO. 1, SEQ ID NO. 2, SEQ ID NO. 3, SEQ ID NO. 9, SEQ ID NO. 11 and SEQ ID NO. 13, by standard techniques of amplification and/or hybridization, and be characterized. The nucleotide sequences according to the invention are preferably obtained by PCR amplification of the genomic DNA of the relevant organism using oligonucleotides I and II. A part-fragment of the relevant sucrose isomerase gene is obtained in this way and can subsequently be used as hybridization probe for isolating the complete gene from a gene bank of the relevant microorganism. Alternatively, the nucleotide sequences can be obtained by producing a gene bank from the particular organism and direct screening of this gene bank with oligonucleotides I, II, III and/or IV.

The present invention further relates to a vector which contains at least one copy of a DNA sequence according to the invention. This vector can be any prokaryotic or eukaryotic vector on which the DNA sequence according to the invention is preferably under the control of an expression signal (promoter, operator, enhancer, etc.). Examples of prokaryotic vectors are chromosomal vectors such as, for example, bacteriophages (for example bacteriophage λ) and extrachromosomal vectors such as, for example, plasmids, with circular plasmid vectors being particularly preferred. Suitable prokaryotic vectors are described, for example, in Sambrook et al., supra, Chapters 1–4.

A particularly preferred example of a vector according to the invention is the plasmid pHWS 88 which harbors a sucrose isomerase gene from Protaminobacter rubrum (with the sequence shown in SEQ ID NO:1) under the control of the regulatable tac promoter. The plasmid pHWS 88 was deposited on Dec. 16, 1993, at the Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSM), Mascheroder Weg 1b, 38124 Braunschweig, Germany, under the deposit number DSM 8824 in accordance with the provisions of the Budapest Treaty.

Two further preferred examples of a vector according to the invention are the plasmids pHWG314 and pHWG315, which harbor a sucrose isomerase gene from Protaminobacter rubrum and Pseudomonas mesoacidophila MX-45, respectively, under the control of a regulatable rhamnose promoter. This promoter is described in Wiese et al. (Arch. Microbiol. 176 (2001):187–196) and Wiese et al. (Appl. Microbiol. 55 (2001), 750–757).

In another preferred embodiment of the present invention, the vector according to the invention is a plasmid which is present in the host cell with a copy number of less than 10, particularly preferably with a copy number of 1 to 2 copies per host cell. Examples of vectors of this type are, on the one hand, chromosomal vectors such as, for example, bacteriophage λ or F plasmids. F plasmids which contain the sucrose isomerase gene can be prepared, for example, by transformation of an E. coli strain which contains an F plasmid with a transposon containing the sucrose isomerase gene, and subsequent selection for recombinant cells in which the transposon has integrated into the F plasmid. One example of a recombinant transposon of this type is the plasmid pHWS 118 which contains the transposon Tn 1721 Tet and was prepared by cloning a DNA fragment containing the sucrose isomerase gene from the above-described plasmid pHWS 88 into the transposon pJOE 105 (DSM 8825).

On the other hand, the vector according to the invention can also be a eukaryotic vector, for example a yeast vector (for example YIp, YEp, etc.) or a vector suitable for higher cells (for example a plasmid vector, viral vector, plant vector). Vectors of these types are familiar to the person skilled in the area of molecular biology so that details thereof need not be given here. Reference is made in this connection in particular to Sambrook et al., supra, Chapter 16.

The present invention further relates to a cell which is transformed with a DNA sequence according to the invention or a vector according to the invention. In one embodiment, this cell is a prokaryotic cell, preferably a Gram-negative prokaryotic cell, particularly preferably an enterobacterial cell. It is moreover possible on the one hand to use a cell which contains no sucrose isomerase gene of its own, such as, for example, E. coli, but it is also possible, on the other hand, to use cells which already contain such a gene on their chromosome, for example the microorganisms mentioned above as source of sucrose isomerase genes. Preferred examples of suitable prokaryotic cells are E. coli, Protaminobacter rubrum or Erwinia rhapontici cells. The transformation of prokaryotic cells with exogenous nucleic acid sequences is familiar to a person skilled in the area of molecular biology (see, for example, Sambrook et al., supra, Chapter 1–4).

In another embodiment of the present invention, the cell according to the invention may, however, also be a eukaryotic cell such as, for example, a fungal cell (for example yeast), an animal or a plant cell. Methods for the transformation or transfection of eukaryotic cells with exogenous nucleic acid sequences are likewise familiar to the person skilled in the area of molecular biology and need not be explained here in detail (see, for example, Sambrook et al., Chapter 16).

The invention also relates to a protein with a sucrose isomerase activity as defined above, which is encoded by a DNA sequence according to the invention. This protein preferably comprises

(a) one of the amino-acid sequences shown in SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:10, SEQ ID NO:12 or SEQ ID NO:14, where appropriate without the signal peptide region or

(b) an amino-acid sequence which is at least 80% homologous with the sequences from (a).

The amino-acid sequence shown in SEQ ID NO:4 comprises the complete sucrose isomerase from Protaminobacter rubrum. The signal peptide extends from amino acid 1–33. The mature protein starts at amino acid 34. The amino-acid sequence shown in SEQ ID NO:5 comprises the N-terminal section of the sucrose isomerase from Erwinia rhapontici. The signal peptide extends from amino acid 1–36. The mature protein starts at amino acid 37. The amino-acid sequence shown in SEQ ID NO:6 comprises a section of the sucrose isomerase from the microorganism SZ 62. FIG. 1 compares the amino-acid sequences of the isomerases from P. rubrum, E. rhapontici and SZ 62.

Amino-acid sequence SEQ ID NO:10 comprises a variant of the isomerase from P. rubrum. Amino-acid sequence SEQ ID NO:12 comprises the complete isomerase from SZ 62. This enzyme has a high activity at 37° C. and produces only a very small proportion of monosaccharides. Amino-acid sequence SEQ ID NO:14 comprises a large part of the isomerase from MX-45. This enzyme produces about 85% trehalulose and 13% palatinose.

The protein according to the invention particularly preferably has an at least 90% homologous amino-acid sequence to conserved part-regions from the amino-acid sequences shown in SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:10, SEQ ID NO:12 or SEQ ID NO:14, especially in part-regions from

(a) amino acid 51–149,

(b) amino acid 168–181,

(c) amino acid 199–250,

(d) amino acid 351–387 and/or

(e) amino acid 390–420

of the amino-acid sequence shown in SEQ ID NO:4.

It is possible by means of the above mentioned DNA sequences, vectors, transformed cells and proteins to provide a sucrose isomerase activity in a simple manner without interfering additional enzymatic activities. Preferably, the sucrose isomerase activity is >30 units/mg and more preferably >45 units/mg. Most preferably the sucrose isomerase activity lies in the range of from 45 units/mg to 150 units/mg.

It is possible for this purpose on the one hand to obtain the sucrose isomerase by recombinant DNA technology as constituent of an extract from the host organism or in isolated and purified form (for example by expression in E. coli). This preferably purified and isolated sucrose isomerase enzyme can be used, for example, in immobilized form, for the industrial production of acariogenic sugars such as, for example, trehalulose and/or palatinose by reaction of sucrose in an enzyme reactor. The immobilization of enzymes is familiar to a skilled person and need not be described in detail here.

On the other hand, the production of acariogenic sugars from sucrose can also take place in a complete microorganism, preferably in immobilized form. Cloning of the abovementioned sucrose isomerase gene into an organism without or with reduced palatinose and/or trehalulose metabolism (that is to say in an organism which is unable significantly to degrade the abovementioned sugars) allows generation of a novel organism which, owing to the introduction of exogenous DNA, is able to produce acariogenic disaccharides with negligible formation of monosaccharides. Thus, suitable for introducing the sucrose isomerase gene is, on the one hand, an organism which is unable to utilize palatinose and/or trehalulose (for example E. coli, bacillus, yeast) and, on the other hand, an organism which would in principle be able to utilize palatinose and/or trehalulose but has reduced palatinose and/or trehalulose metabolism owing to undirected or directed mutation.

The term “reduced palatinose and/or trehalulose metabolism” means for the purpose of the present invention that a whole cell of the relevant organism produces, on utilization of sucrose as C source, acariogenic disaccharides but is able to utilize the latter to only a small extent in metabolism, for example by degrading them to monosaccharides. The organism preferably produces less than 2.5%, particularly preferably less than 2%, most preferably less than 1%, of glucose plus fructose based on the total of acariogenic disaccharides and monosaccharide degradation products at a temperature of 15–65° C., in particular of 25–55° C.

The present invention thus further relates to a cell which contains at least one DNA sequence coding for a protein with a sucrose isomerase activity, and has a reduced palatinose and/or trehalulose metabolism as defined above. Preferably the cell according to the invention exhibits such a sucrose isomerase expression rate that the amount of sucrose isomerase expressed in the cell is >10%, preferably >15% and particularly >25% of the total amount of proteins of the cell. A cell of this type produces larger proportions of the non-cariogenic disaccharides trehalulose and/or palatinose and reduced amounts of the interfering byproducts glucose and fructose.

It is possible in one embodiment of the present invention to reduce the palatinose and/or trehalulose metabolism by partial or complete inhibition of the expression of invertase and/or palatinase genes which are responsible for the intracellular degradation of palatinose and/or trehalulose. This inhibition of gene expression can take place, for example, by site-directed mutagenesis and/or deletion of the relevant genes. A site-directed mutation of the palatinase gene shown in SEQ ID NO:7 or of the palatinose hydrolase gene shown in SEQ ID NO:15 can take place, for example, by introduction of a vector which is suitable for homologous chromosomal recombination and which harbors a mutated palatinase gene, and selection for organisms in which such a recombination has taken place. The principle of selection by genetic recombination is explained in E. L. Winnacker, Gene und Klone, Eine Einführung in die Gentechnologie (1985), VCH-Verlagsgesellschaft Weinheim, Germany, pp. 320 et seq.

It is furthermore possible to obtain organisms according to the invention with reduced palatinose and/or trehalulose metabolism by non-specific mutagenesis from suitable starting organisms and selection for palatinase-deficient mutants. One example of a palatinase-deficient mutant of this type is the Protaminobacter rubrum strain SZZ 13 which was deposited on Mar. 29, 1994, at the Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSM), Mascheroder Weg 1b, 38124 Braunschweig, Germany, under deposit number DSM 9121 in accordance with the provisions of the Budapest Treaty. This microorganism was prepared by non-specific mutagenesis of P. rubrum wild-type cells with N-methyl-N′-nitro-N-nitrosoguanidine and is distinguished in that it is no longer able to cleave the non-cariogenic sugars trehalulose and palatinose to glucose and fructose. Selection for such mutants can take place, for example, by using MacConkey palatinose media or minimal salt media with palatinose or glucose as sole C source. The mutants which are white on MacConkey palatinose medium (MacConkey Agar Base from Difco Laboratories, Detroit, Mich., USA (40 g/l) and 20 g/l palatinose) or which grow on minimal salt media with glucose as sole C source but not on corresponding media with palatinose as sole C source are identified as palatinase-deficient mutants.

The present invention furthermore relates to a method for isolating nucleic acid sequences which code for a protein with a sucrose isomerase activity, wherein a gene bank from a donor organism which contains a DNA sequence coding for a protein with a sucrose isomerase activity is set up in a suitable host organism, the clones of the gene bank are examined, and the clones which contain a nucleic acid coding for a protein with sucrose isomerase activity are isolated. The nucleic acids which are isolated in this way and code for sucrose isomerase can in turn be used for introduction into cells as described, above in order to provide novel producer organisms of acariogenic sugars.

In this method, the chosen host organism is preferably an organism which has no functional genes of its own for palatinose metabolism, in particular no functional palatinase and/or invertase genes. A preferred host organism is E. coli. To facilitate characterization of palatinose-producing clones it is possible on examination of the clones in the gene bank for sucrose-cleaving clones and the DNA sequences which are contained therein and originate from the donor organism to be isolated and transformed in an E. coli strain which does not utilize galactose and which is used as screening strain for the clones in the gene bank.

On the other hand, the examination of the clones in the gene bank for DNA sequences which code for a protein with a sucrose isomerase activity can also take place using nucleic acid probes derived from the sequences SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:9, SEQ ID NO:11 and SEQ ID NO:13 which code for the sucrose isomerase genes from Protaminobacter rubrum, Erwinia rhapontici and the isolate SZ 62. A DNA fragment obtained by PCR reaction with oligonucleotides I and II as primers, or the oligonucleotides III and/or IV, are particularly preferably used as probes.

The present invention further relates to a process for the production of non-cariogenic sugars, in particular trehalulose and/or palatinose, which comprises using for the production of the sugars

-   -   (a) a protein with sucrose isomerase activity in isolated form,     -   (b) an organism which is transformed with a DNA sequence which         codes for protein with sucrose isomerase activity, or with a         vector which contains at least one copy of this DNA sequence,     -   (c) an organism which contains at least one DNA sequence coding         for a protein with a sucrose isomerase activity, and has a         reduced palatinose and/or trehalulose metabolism, and/or     -   (d) an extract from such a cell or from such an organism.

The process is generally carried out by contacting the protein, the organism or the extract in a suitable medium with sucrose under conditions such that the sucrose is at least partly converted by the sucrose isomerase into acariogenic disaccharides. Subsequently, the acariogenic disaccharides are obtained from the medium or the organism and purified in a known manner.

In a preferred embodiment of this process, the organism, the protein or the extract is used in immobilized form. Proteins (in pure form or in extracts) are preferably immobilized by coupling of reactive side groups (for example NH₂ groups) to a suitable carrier. Immobilization of cells takes place, for example, in a sodium alginate/calcium chloride solution. A review of suitable methods for immobilizing cells and proteins is given, for example, in I. Chibata (Immobilized Enzymes, John Wiley and Sons, New York, London, 1978).

It is possible on Use of a cell transformed with the sucrose isomerase gene to increase the rate of production of acariogenic sugars by comparison with known organisms by increasing the number of gene copies in the cell and/or by increasing the expression rate in a combination with strong promoters. It is furthermore possible by transformation of a cell which is unable or able to only a limited extent to utilize acariogenic sugars with the sucrose isomerase gene to produce a transformed cell with whose aid it is possible to obtain acariogenic sugars, in particular palatinose and/or trehalulose, without or with fewer byproducts.

On use of a microorganism with reduced palatinose and/or trehalulose metabolism, which already contains a functional sucrose isomerase gene, transformation with an exogenous sucrose isomerase gene is not essential but may be carried out to improve the yields.

Finally, the present invention also relates to a DNA sequence which codes for a protein with palatinase or palatinose hydrolase activity and comprises

-   -   (a) one of the nucleotide sequences shown in SEQ ID NO:7 or SEQ         ID NO:15,     -   (b) a nucleotide sequence which corresponds to the sequence         from (a) within the scope of the degeneracy of the genetic code         or     -   (c) a nucleotide sequence which hybridizes with the sequences         from (a) and/or (b).

The invention further relates to a vector which contains at least one copy of the above mentioned DNA sequence and to a cell which is transformed with a DNA sequence or a vector as mentioned above. The invention likewise embraces a protein with palatinase activity which is encoded by a DNA sequence as indicated above and which preferably has one of the amino-acid sequences shown in SEQ ID NO:8 or SEQ ID NO:16.

The palatinase from P. rubrum shown in SEQ ID NO:8 differs from known sucrose-cleaving enzymes in that it cleaves the sucrose isomers which are not cleaved by known enzymes in particular palatinose.

The amino acid sequence shown in SEQ ID NO:16 comprises a palatinose hydrolase from MX-45, which cleaves palatinose to form fructose and glucose. The gene-coding for this enzyme is shown in SEQ ID NO:15 and is located in the genome of MX-45 on the 5′ side of the isomerase gene shown in SEQ ID NO:13.

The invention is further described by the following sequence listings and figures:

SEQ ID NO:1 shows the nucleotide sequence of the gene coding for the sucrose isomerase from Protaminobacter rubrum. The sequence coding for the signal peptide terminates at nucleotide No. 99.

SEQ ID NO:2 shows the N-terminal section of the nucleotide sequence of the gene coding for the sucrose isomerase of Erwinia rhapontici. The sequence coding for the signal peptide terminates at the nucleotide with No. 108.

SEQ ID NO:3 shows a section of the nucleotide sequence of the gene coding for the sucrose isomerase from the isolate SZ 62.

SEQ ID NO:4 shows the amino-acid sequence of the sucrose isomerase from Protaminobacter rubrum.

SEQ ID NO:5 shows the N-terminal section of the amino-acid sequence of the sucrose isomerase from Erwinia rhapontici.

SEQ ID NO:6 shows a section of the amino-acid sequence of the sucrose isomerase from the isolate SZ 62.

SEQ ID NO:7 shows the nucleotide sequence for the palatinase gene from Protaminobacter rubrum.

SEQ ID NO:8 shows the amino-acid sequence of the palatinase from Protaminobacter rubrum.

SEQ ID NO:9 shows the nucleotide sequence of a variant of the sucrose isomerase gene from P. rubrum.

SEQ ID NO:10 shows the corresponding amino-acid sequence.

SEQ ID NO:11 shows the complete nucleotide sequence of the sucrose isomerase gene from SZ 62.

SEQ ID NO:12 shows the corresponding amino-acid sequence.

SEQ ID NO:13 shows most of the sucrose isomerase gene from Pseudomonas mesoacidophila (MX-45).

SEQ ID NO:14 shows the corresponding amino acid sequence.

SEQ ID NO:15 shows the palatinose hydrolase gene from Pseudomonas mesoacidophila (MX-45).

SEQ ID NO:16 shows the corresponding amino-acid sequence.

FIG. 1 shows a comparison of the amino-acid sequences of the sucrose isomerases from Protaminobacter rubrum (to the 208^(th) amino acid of SEQ ID NO:4), Erwinia rhapontici (to the 208^(th) amino acid of SEQ ID NO:5) and the isolate SZ 62 (SEQ ID NO:6),

FIG. 2 shows the cloning diagram for the preparation of the recombinant plasmid pHWS 118 which contains the sucrose isomerase gene on the transposon Tn 1721,

FIG. 3 shows the diagram for the preparation of E. coli transconjugants which contain the sucrose isomerase gene of a F plasmid and

FIG. 4 shows a comparison between the saccharides produced by P. rubrum wild-type cells and cells of the P. rubrum mutant SZZ 13.

FIG. 5 shows plasmid pHWG314.

FIG. 6 shows plasmid pHWG315.

The following examples serve to illustrate the present invention.

EXAMPLE 1

Isolation of the Sucrose Isomerase Gene from Protaminobacter rubrum

Complete DNA from the organism Protaminobacter rubrum (CBS 574.77) was partially digested with Sau3A I. Collections of fragments with a size of about 10 kBp were obtained from the resulting fragment mixture by elution after fractionation by gel electrophoresis and were ligated into a derivative, which had been opened with BamHI, of the lambda EMBL4 vector derivative λ RESII (J. Altenbuchner, Gene 123 (1993), 63–68). A gene bank was produced by transfection of E. coli and transformation of the phages into plasmids according to the above reference. Screening of the kanamycin-resistant colonies in this gene bank was carried out with the radiolabeled oligonucleotide S214 which was derived from the sequence of the N terminus of the mature isomerase by hybridization:

S214: 5′-ATCCCGAAGTGGTGGAAGGAGGC-3′ (SEQ ID NO:21)      T  A  A        A  A

Subsequently, the plasmid DNA was isolated from the colonies with a positive reaction after appropriate cultivation. After a restriction map had been drawn up, suitable subfragments were sequenced from a plasmid pKAT 01 obtained in this way, and thus the complete nucleotide sequence, which is shown in SEQ ID NO:1, of the DNA coding for isomerase was obtained. The amino-acid sequence derived therefrom corresponds completely to the peptide sequence of the mature isomerase obtained by sequencing (Edmann degradation). A cleavage site for SacI is located in the non-coding 3′ region of this isomerase gene, and a cleavage site for HindIII is located in the non-coding 5′ region. This makes it possible to subclone the intact isomerase gene into the vector pUCBM 21 (derivative of the vector pUC 12, Boehringer Mannheim GmbH, Mannheim, Germany) which had previously been cleaved with the said enzymes. The resulting plasmid was called pHWS 34.2 and confers on the E. coli cells harboring it the ability to synthesize sucrose isomerase.

A variant of the sucrose isomerase gene from P. rubrum has the nucleotide sequence shown in SEQ ID NO:9.

EXAMPLE 2

Cloning and Expression of the Sucrose Isomerase from P. rubrum in E. coli

1. Preparation of the Plasmid pHWS88

The non-coding 5′ region of the sucrose isomerase gene was deleted from the plasmid pHWS 34.2, using an oligonucleotide S434 with the sequence 5′-CGGAATTCTTATGCCCCGTCAAGGA-3′ (SEQ ID NO:22), with simultaneous introduction of an EcoRI cleavage site (GAATTC). The isomerase gene derivative obtained in this way was treated with BstE II, the protruding BstE II end was digested off with S1 nuclease and subsequently digestion with EcoRI was carried out. The isomerase gene treated in this way was cloned into the vector pBTacl (Boehringer Mannheim GmbH, Mannheim, Germany) which had been pretreated with EcoRI and Smal. The resulting vector pHWS 88 (DSM 8824) contains the modified isomerase gene with a preceding EcoRI restriction site in front of the ATG start codon, and the 3′ region of the isomerase gene up to the S1-truncated BstE II cleavage site. On induction with IPTG, this vector confers on the cells harboring this plasmid the ability to produce isomerase and resistance to ampicillin (50 to 100 μg/ml). Preferably used for producing isomerase are E. coli host cells which overproduce the lac repressor.

2. Preparation of the Plasmid pHWS118::Tn1721Tet

The gene cassette for the sucrose mutase was incorporated into a transposon.

This took place by cloning an Sphl/HindIII DNA fragment from the plasmid pHWS88, which harbors the sucrose mutase gene under the control of the tac promoter, into the plasmid pJOE105 on which the transposon Tn 1721 is located. The plasmid pJOE105 was deposited on Dec. 16, 1993, at the DSM under the deposit number DSM 8825 in accordance with the provisions of the Budapest Treaty. The resulting plasmid pHWS118, on which the sucrose mutase gene is under the control of the regulatable tac promoter, was used to transform a E. coli strain containing an F′ plasmid. FIG. 2 shows the cloning diagram for the preparation of pHWS 118 from pHWS88 and pJOE 105.

E. coli transconjugants containing the sucrose mutase gene were prepared as described in the diagram in FIG. 3. For this purpose, firstly the F′-harboring E. coli strain CSH36 (J. H. Miller, Experiments in Molecular Genetics, Cold Spring Harbor Laboratory (1972), p. 18), which carries the Lac+ phenotype mediated by the F′ plasmid, was crossed with the E. coli strain JM108 which is resistant to nalidixic acid (Sambrook et al., supra, p. A9–A13). Selection on minimal medium to which lactose, proline and nalidixic acid were added resulted in an F′-Lac-harboring transconjugant. This was additionally transformed with the Iq plasmid FDX500 (Brinkmann et al., Gene 85 (1989), 109–114) in order to permit control of the sucrose mutase gene by the tac promoter.

The transconjugant prepared in this way was transformed with the transposon plasmid pHWS118 harboring the sucrose mutase gene. For selection of transconjugants, crossing into the streptomycin-resistant E. coli strain HB101 (Boyer and Roulland-Dussoix, J. Mol. Biol 41 (1969), 459–472) was carried out. Transfer of the tetracycline resistance mediated by the transposon was possible only after transposition of the modified Tn1721Tet from the plasmid pHWS118, which is not capable of conjugation or mobilization, to-the F′ plasmid which is capable of conjugation. Transmission of the F′ plasmid with the modified transposon in HB101 was selected on LB plates containing streptomycin and tetracycline, and retested on ampicillin and nalidixic acid plates.

3. Expression of the Sucrose Isomerase in E. coli

Examination of the enzyme production by such F′ plasmid-harboring E. coli cells showed that it was possible to produce sucrose mutase protein. F′ plasmid-containing HB101 cells which harbored no additional Lac repressor plasmid (for example K1/1 or K1/10) produced sucrose mutase protein in identical amounts with and without the inducer isopropyl β-D-thiogalactoside (IPTG). The productivities of three transconjugants K1/1, K1/10 and K1/4 are shown in Table 1.

It was possible to observe normal growth of the E. coli cells during production of sucrose mutase protein.

Introduction of the sucrose mutase gene into the F

plasmid in the presence of the repressor-encoded plasmid pFDX500 (see transconjugants K1/4) made it possible to control enzyme production with the inducer IPTG. Whereas no enzymatic activity was measured without IPTG, production of about 1.6 U/mg sucrose mutase protein was obtainable after induction for 4 hours.

No adverse effect on cell growth was observable. The plasmid-harboring E. coli cells reached a density of about 3 OD₆₀₀ after induction for 4 hours.

Up to 1.6 U/mg sucrose mutase activity were measured in transformed E. coli. The synthetic performance is comparable to that of P. rubrum. Analysis of the produced enzyme by SDS gel electrophoresis provides no evidence of inactive protein aggregates. The band of the sucrose mutase protein was only weakly visible with Coomassie staining and was detectable clearly only in a Western blot. It was possible to correlate the strength of the protein band and the measured enzymatic activity in the production of sucrose mutase in E. coli.

EXAMPLE 3

Isolation of the Sucrose Isomerase Gene from Erwinia rhapontici

A gene bank was produced by restriction cleavage of the complete DNA from Erwinia rhapontici (NCPPB 1578) in the same way as described in Example 1.

Using the primer mixtures

5′-TGGTGGAAAGAAGCTGT-3′ (SEQ ID NO:23)             G G and 5′-TCCCAGTTCAGGTCCGGCTG-3′, (SEQ ID NO:24)               A PCR amplification resulted in a DNA fragment with whose aid it is possible to identify colonies containing the mutase gene by hybridization.

In this way, a positive clone pSST2023 which contains a fragment, 1305 nucleotides long, of the Erwinia isomerase gene was found. The nucleotide sequence of this fragment is depicted in SEQ ID NO:2.

Sequence comparison with the Protaminobacter gene reveals an identity of 77.7% and a similarity of 78% for the complete gene section including the signal peptide region, and an identity of 83.4% and a similarity of 90.3% at the amino-acid level.

The sequence differences are mainly concentrated in the signal peptide region. For this reason, only the enzyme-encoding region responsible for the actual mutase activity, without the signal peptide, should be considered for comparison. From these viewpoints, the identity or similarity at the nucleotide level emerges as 79%. Comparison of the amino-acid sequences (FIG. 1) in this section shows 87.9% identical amino acids. Of 398 amino acids (this corresponds to 71% of the complete enzyme) in the Erwinia mutase, 349 are the same as in Protaminobacter. 25 of 48 exchanged amino acids show strong similarity so that the overall similarity at the AA level emerges as 94%. The AA exchanges are mainly concentrated in the region between amino acid 141 and 198. In front of this region there is a sequence of 56 conserved amino acids. Other sections also exhibit particularly high conservation (see FIG. 1).

These data show that, for the section cloned and sequenced to date, overall there is very extensive conservation of the two mutases from Erwinia and Protaminobacter.

Identity of the Cloned Mutase Gene from Erwinia

The probe chosen for a rehybridization experiment with genomic Erwinia DNA was the SspI/EcoRI fragment, which is about 500 bp in size, from pSST2023. This fragment was used, after digoxigenin labeling, for hybridization with Erwinia DNA with high stringency (68° C.). Complete Erwinia DNA cut with SspI/EcoRI showed a clear hybridization signal with the expected size of about 500 bp. Erwinia DNA cut only with SspI showed a hybridization signal of about 2 kb.

It was possible to verify by the successful rehybridization of pSST2023 with genomic Erwinia DNA that the mutase region cloned into pSST2023 originates from Erwinia rhapontici.

Cloning of the C-Terminal Part-Fragment of the Erwinia Mutase

The N-terminal part-fragment of the Erwinia mutase gene which has been cloned to date-has a size of 1.3 kb and has the nucleotide sequence shown in SEQ ID NO:2. Since it can be assumed that the complete Erwinia gene is virtually identical in size to the known Protaminobacter gene (1.8 kb), a section of about 500 bp is missing from the C-terminal region of the Erwinia gene.

The SspI fragment which is about 2 kb in size from the complete Erwinia DNA was selected for cloning of the Erwinia C-terminus. In a Southern blot, this fragment provides a clear signal with a digoxigenin-labeled DNA probe from pSST2023. This 2 kb SspI fragment overlaps by about 500 bp at the 3′ end with the region already cloned in pSST2023. Its size ought to be sufficient for complete cloning of the missing gene section of about 500 bp. The digoxigenin-labeled fragment probe SspI/EcoRI from pSST2023 is suitable for identifying clones which are sought.

EXAMPLE 4

Preparation of a Protaminobacter Palatinase-Deficient Mutant

Cells of Protoaminobacter rubrum (CBS 547, 77) were mutagenized with N-methyl-N′-nitro-N-nitroso-guanidine by the method of Adelberg et al. (Biochem. Biophys. Research Commun. 18 (1965), 788) as modified by Miller, J., (Experiments in Molecular Genetics, Cold Spring Harbor Laboratory, 125–179 (1972)). Palatinase-deficient mutants were selected using MacConkey palatinose medium (MacConkey Agar Base (Difco Laboratories, Detroit, Mich., USA), 40 g/l with the addition of 20 g/l palatinose, sterilized by filtration, 25 mg/l kanamycin) and minimal salt media (10.5 g of K₂HPO₄, 4.5 g of KH₂PO₄, 1 g of (NH₄)₂SO₄, 0.5 g of sodium citrate.2 H₂O, 0.1 g of MgSO₄.7H₂O), 1 mg of thiamine, 2 g of palatinose or glucose, 25 mg of kanamycin and 15 g of agar per liter, pH 7.2). Mutants of P. rubrum which are white on MacConkey palatinose medium or grow on minimal salt medium with glucose in contrast to the same medium with palatinose are identified as palatinase-deficient mutants. The enzyme activity of cleaving palatinose to glucose and fructose (palatinase activity) cannot, in contrast to the wild-type, be detected in cell extracts from these mutants. On cultivation of these cells in minimal salt medium with 0.2% sucrose as sole C source there is, in contrast to the wild-type cells in which palatinose can be detected only transiently in the time from 4 to 11 hours after starting the culture, a detectable continuous accumulation of palatinose (isomaltulose). Overnight cultures in the same medium contain no palatinose in the case of the wild-type cells but contain >0.08% palatinose in the case of the mutant SZZ 13 (DSM 9121) prepared in this way (see FIG. 4).

EXAMPLE 5

Immobilization of Microorganism Cells

Cells are rinsed off a subculture of the appropriate strain using 10 ml of a sterile nutrient substrate composed of 8 kg of concentrated juice from a sugar factory (dry matter content=65%), 2 kg of corn steep liquor, 0.1 kg of (NH₄)₂HPO₄ and 89.9 kg of distilled water, pH 7.2. This suspension is used as inoculum for preculture in 1 l flasks containing 200 ml of nutrient solution of the above composition in shaking machines. After an incubation time of 30 hours at 29° C., 10 flasks (total contents 2 l) are used to inoculate 18 l of nutrient solution of the above composition in a 30 l small fermenter, and fermentation is carried out at 29° C. and a stirring speed of 350 rpm introducing 20 l of air per minute.

After organism counts above 5×10⁹ organisms per ml are reached, the fermentation is stopped and the cells are harvested from the fermenter solution by centrifugation. The cells are then suspended in a 2% strength sodium alginate solution and immobilized by dropwise addition of the suspension to a 2% strength calcium chloride solution. The resulting immobilizate beads are washed with water and can be stored at +4° C. for several weeks.

Cells of the palatinase-deficient mutant SZZ 13 (DSM 9121) show better catalytic properties in respect of their product composition than do comparable cells from the known microorganisms Protaminobacter rubrum (CBS 547.77) and Erwinia rhapontici (NCPPB 1578).

Whole cells and crude extracts of SZZ 13, and an immobilizate of SZZ 13 in calcium alginate prepared as above, were evaluated in respect of product composition in an activity assay. Before the actual activity assay, the immobilizate was swollen in 0.1 mol/l potassium phosphate buffer, pH 6.5.

The activity measurements at 25° C. revealed that no fructose and glucose were found with the mutant SZZ 13, while with P. rubrum wild-type cells 2.6% fructose and glucose (based on the total of mono- and disaccharides) were found in whole cells and 12.0% were found in the crude extract. In the case of E. rhapontici, 4% glucose and fructose were found in whole cells, and 41% in the crude extract.

EXAMPLE 6

Isolation of the Sucrose Isomerase Gene from other Microorganisms

Partial digestion of genomic DNA from the isolate SZ62 (Enterobacter spec.), the organism Pseudomonas mesoacidophila (MX-45) or from another microorganism and insertion of the resulting fragments into suitable E. coli vectors and transformation result in a gene bank whose clones contain genomic sections between 2 and 15 kb of the donor organism.

Those E. coli cells which harbor these plasmids and which display a red coloration of the colony are selected by plating on McConkey palatinose medium. The plasmid DNA contained in these cells is transferred into an E. coli mutant which is unable to grow on galactose as sole C source (for example ED 8654, Sambrook et al., supra, pages A9–A13).

This transformed cell line is able to identify palatinose producers in the gene bank which has been prepared as described above from DNA of the donor organism.

To identify the palatinose-producing clones which are sought, the cells of the gene bank are isolated and cultured on minimal salt media containing galactose and sucrose. After replica plating of the colonies on plates containing the same medium, the cells are killed by exposure to toluene vapor. Subsequently, cells of the screening strain are spread as lawn in minimal salt soft agar without added C source over the colonies of the gene bank and incubated. Significant growth of the cells of the screening strain appears only at the location of cells in the gene bank which have produced palatinose. The isomerase content emerges on testing the cells of the replica control.

These E. coli clones identified in this way are unable to grow on palatinose as sole C source in the medium, show no ability to cleave sucrose in a test on whole cells or on cell extracts, but on cultivation under these conditions and without addition of sucrose to the medium produce palatinose.

Alternatively, isomerase clones can,also be identified using a PCR fragment prepared by the procedure of Example 3.

Use of plasmid DNA from the E. coli clones identified in this way as probes for hybridization on filters with immobilized DNA from the donor organism allows the gene regions which harbor isomerase genes to be detected and specifically made available.

A clone which contains the nucleotide sequence shown in SEQ ID NO:3, with the amino-acid sequence which, is derived therefrom and shown in SEQ ID NO:6, was identified in this way. In the same way an isomerase clone from DNA of the bacterial strain Pseudomonas mesoacidophila MX-45 (FERM 11808) was found.

The complete nucleotide sequence and amino-acid sequence of the sucrose isomerase from SZ 62 are depicted in SEQ ID NO:11 and 12. A large part of the nucleotide sequence and amino-acid sequence of the sucrose isomerase from MX-45 are depicted in SEQ ID NO:13 and 14.

EXAMPLE 7

Cloning of a Palatinase Gene

The Protaminobacter rubrum gene bank prepared in Example 1 was screened with the radiolabeled oligonucleotide mixture S433 which was derived from the sequence of the N-terminus of the isolated palatinase and had the sequence CA(G,A)TT(C,T)GG(T,C)TA(C,T)GG-3′ (SEQ ID NO:25).

A positive clone was found, and a plasmid named pKAT 203 was isolated therefrom.

E. coli cells which harbor the plasmid pKAT 203 are able to metabolize palatinose. The cleavage of palatinose to glucose and fructose which is detectable in the activity assay suggests that there is a “palatinase”.

It is possible by sequencing pKAT203 DNA with the oligonucleotide S433 as primer to obtain a DNA sequence from which it was possible to read off, after translation into amino-acid sequence data, the N-terminal amino acids known to us. An open reading frame was obtained by a subsequent sequencing step.

Determination of the Sequence of the “Palatinase” Gene

For further sequencing of the “palatinase” gene, part-fragments from the plasmid pKAT 203 were selected on the basis of the restriction map and subcloned in the M13 phage system, and a sequencing of the single-stranded phage DNA was carried out with the universal primer 5′-GTTTTCCCAGTCACGAC-3′ (SEQ ID NO:26).

Combination of the resulting DNA sequence data for the individual fragments taking account of overlapping regions allows a continuous reading frame of 1360 base pairs to be determined for the “palatinase” (SEQ ID NO:7).

Translation of this DNA sequence into amino-acid data reveals a protein with 453 amino acids (SEQ ID NO:8) and a molecular weight, which can be deduced therefrom, of about 50,000 Da. This is consistent with the finding that a protein fraction which had a band at about 48,000 Da in the SDS gel was obtainable by concentration of the “palatinase” activity. In the native gel, the palatinose-cleaving activity was attributable to a band with a size of about 150,000 Da.

Comparisons of Homology with other Known Proteins

Comparison of the amino-acid sequence derivable from the DNA sequence with data stored in a gene bank (SwissProt) revealed a homology with melibiase from E. coli (MelA) (in two parts: identity 32%).

EXAMPLE 8

Cloning of a Palatinose Hydrolase Gene from P. mesoacidophila MX-45

A gene with the nucleotide sequence shown in SEQ ID NO:15 was isolated from the gene bank prepared from the microorganism P. mesoacidophila MX-45 in Example 6. This gene codes for a protein with the amino-acid sequence shown in SEQ ID NO:16. The protein is a palatinose hydrolase which catalyzes the cleavage of palatinose to form fructose and glucose.

EXAMPLE 9

Cloning and Expression of the Sucrose Isomerase from Protaminobacter rubrum and Pseudomonas mesoacidophila MX-45 in E. coli

1. Preparation of the Plasmids pHWG314 and pHWG315

The plasmids were prepared by inserting the gene modules into the vector pJOE2702 (Wiese et al. (2001) supra) digested with Ndel/HindIII (314) and Ndel/BamHI (315), respectively. The plasmids carry the entire sequence coding for each mutase. FIGS. 5 and 6 show the restriction maps of both plasmids. E. coli JM109 was used as host.

2. Expression of the Sucrose Isomerase in E. coli and Isolation

The production of the enzyme was induced by adding 0.2% rhamnose to the medium. The cells were harvested via centrifugation and sonification. Standard conditions were applied, as described in the other examples. For the purification from E. coli a chromatography of the raw extract was performed using a cation exchange chromatography column, e.g. a MonoS column (Pharmacia). The material was loaded on the column in the presence of 10 mM Ca-acetate, pH 6.5. The elution was carried out with a NaCl gradient of from 0–100 mM. Then the fractions were tested for their protein content. All results are contained in Table 2.

3. Isolation of the Sucrose Isomerase from Protaminobacter rubrum and Pseudomonas mesoacidophila MX-45

The enzymes from the (wild-type) strains Protaminobacter rubrum and Pseudomonas mesoacidophila were not purified. Purification according to the above protocol was successful only regarding the enzymes produced in E. coli.

After cultivation in a suitable complete medium containing 2% sucrose the cells of the wild-type strains were harvested at 30° C. and decomposed. Then the enzymatic activity and the protein content were determined.

Surprisingly, the recombinant sucrose isomerase can be separated by a one-step procedure from homologous proteins in the E. coli extract exhibiting high yield and purity. Apparently the recombinant protein has a different charge composition compared to the isomerase from native organisms.

A comparison of the results shown in Table 2 shows that with the help of the recombinant E. coli strains significantly higher sucrose isomerase yields can be obtained than with the wild-type strains Pseudomonas mesoacidophila MX-45 and Protominobacter rubrum. The amount of recombinant sucrose isomerase expressed in the E. coli strains is about 15.6 and 28.9%, respectively, of the total amount of proteins in the cell. Contrary thereto, the amount of sucrose isomerase formed in the wild-type strains Pseudomonas mesoacidophila MX-45 and Protominobacter rubrum was so small that it could not be detected by using conventional detection methods. Furthermore, the activity of the recombinant sucrose isomerase is about 10-times higher than the activity of the sucrose isomerase formed in the respective wild-type strains. Consequently, the protein isolated from the wild-type strains must have been inactivated to a great extent when isolated from the wild-type strains.

TABLE 1 Surose mutase activity in E. coli HB101 (F′::Tn1721 [Mutase]) U/mg mutase after 4 hours U/mg mutase after 4 hours Strain without induction induction with 50 μM IPTG K1/1 1.0 1.2 K1/10 0.9 1.1 K1/4 0 1.6

TABLE 2 The results obtained under items 3 and 4 of example 9 are summarized in the following table: Expression Culture pure in E. coli Vol. U mg U in U U in % cell (plasmid) Wild-type strain Gene (ml) OD₆₀₀ ml⁻¹ ml⁻¹ mg ml⁻ (total) mg⁻¹ protein P. mesoacidophila mutB 400 4.0 4.3 0.48 9.0 1.720 n.m. u.m MX-45 pHWG315 mutB 400 3.8 45.2 0.46 98.3 18.080 340 28.9% P. rubrum smuA 400 3.0 1.6 0.36 4.4 640 n.m. u.m pHWG314 smuA 400 2.8 16.5 0.34 48.5 6.600 310 15.6% P. mesoacidophila mutB 3000 27.2 28.4 3.26 8.7 85.200 n.m. u.m. MX-45 pHWG315 mutB 3000 26.6 308.5 3.19 96.7 925.500 n.m. n.m. P. rubrum smuA 3000 29.5 14.9 3.54 4.2 44.700 n.m. u.m. pHWG314 smuA 3000 26.1 149.6 3.13 47.8 448.800 n.m. n.m. n.m. = not measured u.m. = unmeasurable 

1. An isolated or purified polypeptide having palatinase activity, trehalulase activity, or both, that is encoded by a DNA sequence comprising (a) a nucleotide sequence of SEQ ID NO:7 or SEQ ID NO:15, (b) a nucleotide sequence from (a) within the scope of the degeneracy of the genetic code, or (c) a nucleotide sequence that specifically hybridizes with the sequence of (a), (b), or both (a) and (b), wherein a positive hybridization signal is still observed after washing with a stringency of at least 1×SSC and 0.1% SDS at 55° C. for one hour.
 2. The isolated or purified polypeptide as claimed in claim 1, wherein the polypeptide comprises an amino acid sequence of SEQ ID NO:8 and SEQ ID NO:16. 